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Intercellular Adhesion Molecular-5 as Marker in HIV Associated Neurocognitive Disorder

Despite the use of antiretroviral drugs HIV associated neurocognitive disorders (HAND) are still common in HIV-seropositive patients. Identification of HIV patients with cognitive impairment in early-stage might benefit a great deal from disease progression monitoring and treatment adjustment. Inter...

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Autores principales: Yuan, Lin, Wei, Feili, Zhang, Xin, Guo, Xianghua, Lu, Xiaofan, Su, Bin, Zhang, Tong, Wu, Hao, Chen, Dexi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JKL International LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440105/
https://www.ncbi.nlm.nih.gov/pubmed/28580181
http://dx.doi.org/10.14336/AD.2016.0918
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author Yuan, Lin
Wei, Feili
Zhang, Xin
Guo, Xianghua
Lu, Xiaofan
Su, Bin
Zhang, Tong
Wu, Hao
Chen, Dexi
author_facet Yuan, Lin
Wei, Feili
Zhang, Xin
Guo, Xianghua
Lu, Xiaofan
Su, Bin
Zhang, Tong
Wu, Hao
Chen, Dexi
author_sort Yuan, Lin
collection PubMed
description Despite the use of antiretroviral drugs HIV associated neurocognitive disorders (HAND) are still common in HIV-seropositive patients. Identification of HIV patients with cognitive impairment in early-stage might benefit a great deal from disease progression monitoring and treatment adjustment. Intercellular adhesion molecule-5 (ICAM5), characteristically expressed on neuron, may suppress immune functions by inhibition of T cell activation in central nervous system. Previous studies have shown that ICAM5 could be detected in patients with brain injury. To investigate the relationship between cognitive impairment and ICAM5 in HIV patients, we compared soluble ICAM5 levels in paired CSF and plasma specimens from HIV-infected individuals with or without neurocognitive impairment. sICAM5 concentrations were measured by ICAM5 ELISA kit. A total of 41 Patients were classified into HIV infected with normal cognition (HIV-NC) and impaired cognition groups (HIV-CI) based on Memorial Sloan-Kettering Scale. CSF and plasma levels of sICAM5 in HIV-CI patients were significantly higher than HIV-NC group (p<0.0001, p=0.0054 respectively). sICAM5 concentrations in plasma strongly correlated with sICAM5 in CSF (r=0.7250, p<0.0001) and S100B in CSF (r=0.3812, p<0.0139). Among 6 follow-up patients we found that sICAM5 levels in CSF and plasma might change consistently with HAND progression. In summary, we have shown that the expressions of sICAM5 in CSF and plasma may correlate with neurocognitive impairment in HIV infected patients. The elevation of sICAM5 in plasma were correspond with that in CSF as a consequence of blood-brain barrier permeability changes. ICAM5 can serve as a potential and readily accessible biomarker to predict HIV associated neurocognitive disorder.
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spelling pubmed-54401052017-06-02 Intercellular Adhesion Molecular-5 as Marker in HIV Associated Neurocognitive Disorder Yuan, Lin Wei, Feili Zhang, Xin Guo, Xianghua Lu, Xiaofan Su, Bin Zhang, Tong Wu, Hao Chen, Dexi Aging Dis Short Communications Despite the use of antiretroviral drugs HIV associated neurocognitive disorders (HAND) are still common in HIV-seropositive patients. Identification of HIV patients with cognitive impairment in early-stage might benefit a great deal from disease progression monitoring and treatment adjustment. Intercellular adhesion molecule-5 (ICAM5), characteristically expressed on neuron, may suppress immune functions by inhibition of T cell activation in central nervous system. Previous studies have shown that ICAM5 could be detected in patients with brain injury. To investigate the relationship between cognitive impairment and ICAM5 in HIV patients, we compared soluble ICAM5 levels in paired CSF and plasma specimens from HIV-infected individuals with or without neurocognitive impairment. sICAM5 concentrations were measured by ICAM5 ELISA kit. A total of 41 Patients were classified into HIV infected with normal cognition (HIV-NC) and impaired cognition groups (HIV-CI) based on Memorial Sloan-Kettering Scale. CSF and plasma levels of sICAM5 in HIV-CI patients were significantly higher than HIV-NC group (p<0.0001, p=0.0054 respectively). sICAM5 concentrations in plasma strongly correlated with sICAM5 in CSF (r=0.7250, p<0.0001) and S100B in CSF (r=0.3812, p<0.0139). Among 6 follow-up patients we found that sICAM5 levels in CSF and plasma might change consistently with HAND progression. In summary, we have shown that the expressions of sICAM5 in CSF and plasma may correlate with neurocognitive impairment in HIV infected patients. The elevation of sICAM5 in plasma were correspond with that in CSF as a consequence of blood-brain barrier permeability changes. ICAM5 can serve as a potential and readily accessible biomarker to predict HIV associated neurocognitive disorder. JKL International LLC 2017-05-02 /pmc/articles/PMC5440105/ /pubmed/28580181 http://dx.doi.org/10.14336/AD.2016.0918 Text en Copyright: © 2017 Yuan, et al. http://creativecommons.org/licenses/by/2.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Short Communications
Yuan, Lin
Wei, Feili
Zhang, Xin
Guo, Xianghua
Lu, Xiaofan
Su, Bin
Zhang, Tong
Wu, Hao
Chen, Dexi
Intercellular Adhesion Molecular-5 as Marker in HIV Associated Neurocognitive Disorder
title Intercellular Adhesion Molecular-5 as Marker in HIV Associated Neurocognitive Disorder
title_full Intercellular Adhesion Molecular-5 as Marker in HIV Associated Neurocognitive Disorder
title_fullStr Intercellular Adhesion Molecular-5 as Marker in HIV Associated Neurocognitive Disorder
title_full_unstemmed Intercellular Adhesion Molecular-5 as Marker in HIV Associated Neurocognitive Disorder
title_short Intercellular Adhesion Molecular-5 as Marker in HIV Associated Neurocognitive Disorder
title_sort intercellular adhesion molecular-5 as marker in hiv associated neurocognitive disorder
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440105/
https://www.ncbi.nlm.nih.gov/pubmed/28580181
http://dx.doi.org/10.14336/AD.2016.0918
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